Evidence map›Paper›PMID 36712035›Full record

ArticlebioRxiv : the preprint server for biology2023

Measuring prion propagation in single bacteria elucidates mechanism of loss.

Krista Jager, Maria Teresa Orozco-Hidalgo, Benjamin Lennart Springstein, Euan Joly-Smith, Fotini Papazotos, EmilyKate McDonough, Eleanor Fleming, Giselle McCallum, Andreas Hilfinger, Ann Hochschild and 1 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Krista JagerDepartment of Biology, Concordia University, Montréal, Québec, Canada.
Maria Teresa Orozco-HidalgoDepartment of Biology, Concordia University, Montréal, Québec, Canada.
Benjamin Lennart SpringsteinDepartment of Microbiology, Harvard Medical School, Boston, Massachusetts, USA.
Euan Joly-SmithDepartment of Physics, University of Toronto, Toronto, Ontario, Canada.
Fotini PapazotosDepartment of Biology, Concordia University, Montréal, Québec, Canada.
EmilyKate McDonoughDepartment of Microbiology, Harvard Medical School, Boston, Massachusetts, USA.
Eleanor FlemingDepartment of Microbiology, Harvard Medical School, Boston, Massachusetts, USA.
Giselle McCallumDepartment of Biology, Concordia University, Montréal, Québec, Canada.
Andreas HilfingerDepartment of Physics, University of Toronto, Toronto, Ontario, Canada.
Ann HochschildDepartment of Microbiology, Harvard Medical School, Boston, Massachusetts, USA.
Laurent Potvin-TrottierDepartment of Biology, Concordia University, Montréal, Québec, Canada.
Concordia University · CAHarvard University · USUniversity of Toronto · CA

Funding

Prions in the bacterial domain of lifeR35GM136247 · NIGMS · HARVARD MEDICAL SCHOOL · PI Ann Hochschild · 2020 to 2026
$3.2M
NIGMS NIH HHS R35 GM136247
6 · The paper itself

Abstract

Prions are self-propagating protein aggregates formed by specific proteins that can adopt alternative folds. Prions were discovered as the cause of the fatal transmissible spongiform encephalopathies in mammals, but prions can also constitute non-toxic protein-based elements of inheritance in fungi and other species. Prion propagation has recently been shown to occur in bacteria for more than a hundred cell divisions, yet a fraction of cells in these lineages lost the prion through an unknown mechanism. Here, we investigate prion propagation in single bacterial cells as they divide using microfluidics and fluorescence microscopy. We show that the propagation occurs in two distinct modes with distinct stability and inheritance characteristics. We find that the prion is lost through random partitioning of aggregates to one of the two daughter cells at division. Extending our findings to prion domains from two orthologous proteins, we observe similar propagation and loss properties. Our findings also provide support for the suggestion that bacterial prions can form more than one self-propagating state. We implement a stochastic version of the molecular model of prion propagation from yeast and mammals that recapitulates all the observed single-cell properties. This model highlights challenges for prion propagation that are unique to prokaryotes and illustrates the conservation of fundamental characteristics of prion propagation across domains of life.

Identifiers

PMID36712035
PMCPMC9882039
OpenAlexW4315767675

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.